Author

G. A. Joseph

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Cell Biology· 1 Physiology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Research Focus:cancer & tumor microenvironment· 1 Research Focus:host-pathogen & immune response· 1 Organism:mouse· 1 Organism:rat· 1

Frequent Co-Authors

A. B. Madsen· 1 shared A.-M. Lundsgaard· 1 shared D. J. Glass· 1 shared E. A. Richter· 1 shared G. Kimble· 1 shared H. Tse· 1 shared J. K. Eash· 1 shared J. R. Knudsen· 1 shared

Activity by Year

2019-2019 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperCell Biology

A. B. Madsen

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2 papers

Recent·Most cited

Insulin-stimulated glucose uptake partly relies on p21-activated kinase (PAK)-2, but not PAK1, in mouse skeletal muscle

L. L. V. Moller, M. Jaurji, R. Kjobsted, G. A. Joseph, A. B. Madsen, J. R. Knudsen, A.-M. Lundsgaard, N. R. Andersen, P. Schjerling, T. E. Jensen, R. S. Krauss, E. A. Richter, L. Sylow

This study investigates the role of PAK1 and PAK2 in insulin-stimulated glucose uptake in mouse skeletal muscle, finding that PAK2, not PAK1, contributes to this process.

bioRxiv · Dec 16, 2019Cell Biology

Inhibition of mTORC1 signaling in aged rats counteracts the decline in muscle mass and reverses multiple parameters of muscle signaling associated with sarcopenia

G. A. Joseph, S. Wang, W. Zhou, G. Kimble, H. Tse, J. K. Eash, T. Shavlakadze, D. J. Glass

This study shows that inhibiting mTORC1 signaling in aged rats increases muscle mass and reverses sarcopenia-related gene expression changes.

bioRxiv · Mar 28, 2019Physiology